N-methylpiperidine

CC(COc1ccc(C#N)cc1)NC(=O)[C@@H](NC(=O)Oc1ccccc1)C(C)C
Reaction #1025
white powder
المردود 14.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N=C(NC(=O)OCC(Cl)(Cl)Cl)c1cccc(CN2CC[C@H](NS(=O)(=O)c3cc4c(Cl)cc(Cl)cc4s3)C2=O)c1
Reaction #2848
title compound
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOc1cc(C(CC(=O)NOC)N2Cc3ccccc3C2=O)ccc1OC
Reaction #9930
3-(3-ethoxy-4-methoxyphenyl)-N-methoxy-3-(1-oxoisoindolinyl)-propionamide
المردود 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(C(C)NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)cc1
Reaction #64239
N-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamide
المردود 217.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1c(C(C)NC(=O)C(NC(=O)OC(C)(C)C)C(C)C)sc2ccccc12
Reaction #176820
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N=C(NC(=O)OCC(Cl)(Cl)Cl)c1cccc(CN2CCC(NS(=O)(=O)c3cc4c(Cl)cc(Cl)cc4s3)C2=O)c1
Reaction #191311
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(NC(=O)C(NC(=O)Oc1ccccc1)C(C)C)c1nc2cc(Cl)ccc2s1
Reaction #197681
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(N2CC(F)C(C3(NC(=O)OC(C)(C)C)CC3)C2)c(F)c(N)c2c(=O)c(C(=O)O)cn(C3CC3F)c12
Reaction #200213
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(COc1ccc([N+](=O)[O-])cc1)NC(=O)C(NC(=O)OC(C)(C)C)C(C)C
Reaction #203532
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(C)C(NC(=O)OC(C)(C)C)C(=O)NC(C)COc1ccc(C#N)cc1
Reaction #230737
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(NC(=O)C(NC(=O)OC(C)(C)C)C(C)C)C(=O)N(C)c1ccc(Cl)cc1
Reaction #233179
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CON(C)C(=O)c1cc(S(N)(=O)=O)sc1Cl
Reaction #236737
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)OC(=O)NC(C(=O)NC(C)c1cc2cc(F)ccc2o1)C(C)C
Reaction #258152
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(COCc1ccc(Cl)cc1)NC(=O)C(NC(=O)OC(C)C)C(C)C
Reaction #270005
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)OC(=O)NC(C(=O)NCC(=O)Nc1ccc(C#N)cc1)C(C)C
Reaction #276361
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(NC(=O)C(NC(=O)OC(C)(C)C)C(C)C)c1c[nH]c2ccccc12
Reaction #282999
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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Reaction #310787
89
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_10
COc1ccc(C(C)NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)cc1
Reaction #335505
N-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamide
المردود 217.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CON(C)C(=O)[C@H]1C[C@@H](CC(=O)OC(C)(C)C)C1
Reaction #358530
product
المردود 99.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CON(C)C(=O)[C@H]1CC[C@@H](CNC(=O)OC(C)(C)C)CC1
Reaction #358543
tert-butyl [(cis-4-{[methoxy(methyl)amino]carbonyl}cyclohexyl)methyl]carbamate
المردود 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
الصفحة 1التالي